Bioavailability, toxicity and biotransformation of selenium in midge (Chironomus dilutus) larvae exposed via water or diet to elemental selenium particles, selenite, or selenized algae.

Elemental selenium (Se) is generally considered to be biologically inert due to its insolubility in water. It is a common form of Se in sediment near uranium mining and milling operations in northern Saskatchewan, Canada. Nanosized particles of many materials exhibit different properties compared with their bulk phases, in some cases posing health and ecological risks. Here we investigated the bioavailability and toxicity of Se nanoparticles (SeNPs) using 10-day waterborne and dietary exposures to larvae of Chironomus dilutus, a common benthic invertebrate. For comparison, larvae were also exposed to waterborne dissolved selenite and to dietary selenomethionine as selenized algae. Larval Se accumulation was evaluated using graphite furnace atomic absorption spectroscopy or inductively coupled plasma mass spectroscopy for total Se and X-ray absorption spectroscopy for Se chemical speciation. Exposure to nanoparticulate Se resulted in Se bioaccumulation, at high concentrations, inhibiting larval growth in both waterborne and dietary exposures; larvae predominantly accumulated selenomethionine-like species regardless of uptake route or form of Se tested. Despite the observed Se accumulation, our findings suggest there is little risk of direct SeNP toxicity to benthic invertebrates in Se-contaminated sediments in northern Saskatchewan. Nevertheless, elemental Se in sediments may be biologically available and may contribute directly or indirectly to the risk of Se toxicity to egg-laying vertebrates (fish and piscivorous birds) in Se-contaminated aquatic systems. It thus may be necessary to include elemental Se as a source of potential Se exposure in ecological risk assessments.

Focused ultrasound and molecularly imprinted polymers: a new approach to organotin analysis in environmental samples.

There is a high interest in speciation of organotin compounds (OTCs) in biota and marine sediment samples, due to their influence in the transmission of the contamination in the trophic chain. Sample treatment is still the most "compromising" step of speciation analysis. Extraction methods are in general time-consuming due to long extraction times and several analytical steps involved. In addition, in most cases there are problems of low recovery, especially for MBT. These drawbacks, added to the high matrix effects generally present in biota samples, make the sample treatment for organotin analysis a serious challenge for environmental issues. Here we present a novel, fast and efficient two steps method for organotin speciation in mussel and oyster tissue as well as in marine sediments. The first step based on the use of ultrasonic probe extraction for species leaching allowed us to quantitatively extract these compounds in a few minutes. Matrix interferences drastically decreased by applying a clean-up step based on the use of an imprinted polymer especially designed for tributyltin (TBT). This procedure increased accuracy and precision of the GC-FPD analysis and improving the limit of detection, Besides, this new method prevents the use of standard addition calibration method, which is mandatory without the clean-up step. The optimization and validation has been performed by using three reference materials: mussel tissue CRM-477, oyster candidate T-38 and sediment PACS-2.

Transformation of tributyltin in zebrafish eleutheroembryos (Danio rerio).

Organotin compounds are highly versatile group of organometallic chemicals used in industrial and agricultural applications. Their endocrine-disrupting effects are well known and their extensive uses as biocide materials, e.g., in antifouling paints, for many years have led to serious environmental problems. So far, attention has mainly been given to tributyltin pollution in water, sediments, and marine organisms because of its highly toxic effects and high accumulation levels at very low concentrations. In this study, we will focus on the conversion of tributyltin after it is absorbed by zebrafish eleutheroembryos, presented here as an alternative model to adult fish for describing bioconcentration. A simplified analytical extraction procedure based on the use of an assisted ultrasonic probe and derivatization by ethylation, followed by gas chromatography with a flame photometric detector (GC-FPD) is proposed. This classical methodology for organotin determination has been validated by inductively coupled plasma mass spectrometry (ICP-MS) and Zeeman graphite furnace atomic absorption spectrometry (ZGF-AAS) in terms of total tin content. The speciation analysis results show that zebrafish eleutheroembryos absorb high amounts of tributyltin and convert it into monobutyltin and likely in inorganic tin.

An in situ assessment of selenium bioaccumulation from water-, sediment-, and dietary-exposure pathways using caged Chironomus dilutus larvae.

An in situ caging study was conducted downstream of a metal mine in northern Canada to determine the significance of surface water versus sediment exposure on selenium (Se) bioaccumulation in the benthic invertebrate Chironomus dilutus. Laboratory-reared C. dilutus larvae were exposed to either site-specific whole-sediment and surface water or surface water only for 10 d at sites with differing sediment and Se characteristics. Results showed elevated whole-body Se concentrations in C. dilutus larvae when exposed to sediment and water, compared with larvae exposed to Se in the surface water only at concentrations ranging from <1 µg Se/L to 12 µg Se/L. In response to these findings, a second in situ experiment was conducted to investigate the importance of dietary Se (biofilm and detritus) versus whole-sediment-exposure pathways. Larvae exposed to sediment detritus had the highest Se concentrations after 10 d of exposure (15.6 ± 1.9 µg/g dry wt) compared with larvae exposed to whole-sediment (12.9 ± 1.7 µg/g dry wt) or biofilm (9.9 ± 1.6 µg/g dry wt). Detritus and biofilm appear to be enriched sources of organic Se, which are more bioaccumulative than inorganic Se. Midge larvae from the reference treatment contained elevated concentrations of diselenides (i.e., selenocystine), while larvae from the biofilm treatment had the highest concentrations of selenomethionine-like compounds, which may be a biomarker of elevated Se exposures derived from anthropogenic sources. Whenever possible, Se concentrations in the organic fraction of sediment should be measured separately from whole-sediment Se and used for more accurate ecological risk assessments of potential Se impacts on aquatic ecosystems.

Selenium speciation and localization in chironomids from lakes receiving treated metal mine effluent.

A lake system in northern Saskatchewan receiving treated metal mine and mill effluent contains elevated levels of selenium (Se). An important step in the trophic transfer of Se is the bioaccumulation of Se by benthic invertebrates, especially primary consumers serving as a food source for higher trophic level organisms. Chironomids, ubiquitous components of many northern aquatic ecosystems, were sampled at lakes downstream of the milling operation and were found to contain Se concentrations ranging from 7 to 80 mgkg(-1)dry weight. For comparison, laboratory-reared Chironomus dilutus were exposed to waterborne selenate, selenite, or seleno-DL-methionine under laboratory conditions at the average total Se concentrations found in lakes near the operation. Similarities in Se localization and speciation in laboratory and field chironomids were observed using synchrotron-based X-ray fluorescence (XRF) imaging and X-ray absorption spectroscopy (XAS). Selenium localized primarily in the head capsule, brain, salivary glands and gut lining, with organic Se species modeled as selenocystine and selenomethionine being the most abundant. Similarities between field chironomids and C. dilutus exposed in the laboratory to waterborne selenomethionine suggest that selenomethionine-like species are most readily accumulated, whether from diet or water.

A new application of imprinted polymers: speciation of organotin compounds.

Molecular imprinting technology has been employed for the first time to prepare a specifically affinity chromatographic stationary phase for speciation purposes. Tributyltin has been chosen as the template molecule and the non-covalent approach has been applied. Three different polymerization methods have been evaluated: (i) a composite material, (ii) a polymer prepared via-Iniferter grafting; (iii) an emulsion polymer. Columns packed with different polymers have been evaluated by liquid chromatography (LC) coupled to inductively coupled plasma mass spectrometry (ICP-MS). The chromatographic conditions as well as the analytical characteristics of the developed method are discussed in this paper. Our findings have shown formation of specific cavities in the grafted Iniferter as well as in the emulsion polymers with the latter achieving resolution of four organotin compounds. Detection limits are similar to those obtained with commercial, but not specific, stationary phases (6 pg for monobutyltin, MBT; 10 pg for both tributyltin, TBT, and triphenyltin, TPhT; and 20 pg for dibutyltin, DBT). The main advantage of this proposed stationary phase is that good recovery is obtained for all species, including MBT. Baseline resolution for TBT and TPhT has also been obtained. The high selectivity of this column prevents matrix interferences. The method has been validated by analyzing two biota reference materials (ERM-CE477 mussel tissue and T-38 oyster tissue).

Different formats of imprinted polymers for determining organotin compounds in environmental samples.

Organotin compounds and their degradation products enter the environment mainly as a result of their use as biocides and antifouling paints. Analysis of these compounds in environmental samples has to be very sensitive and selective so that their concentrations corresponding to the low environmental target values can also be detected. Generally, analysis of a complex matrix leads to high interferences during the different process steps; clean-up procedures are recommended to overcome this problem. For the past many years, solid phase extraction by employing imprinted materials has been extensively used for many organic substances that are used for pre-concentration and clean-up purposes with excellent results. Here, we present three different imprinted polymers prepared via bulk, precipitation, and emulsion polymerization methods that use similar compositions. The synthesized polymer particles were characterized morphologically by employing scanning electron microscopy and Brunauer-Emmett-Teller analysis. Binding properties were calculated using the Langmuir-Freundlich isotherm. Depending on the properties of the materials, different analytical applications for complex matrices are proposed. These applications are mainly used on tributyltin and its degradation products for environmental analysis.

Synthesis of a pH dependent covalent imprinted polymer able to recognize organotin species.

The covalent imprinting approach has for the first time been successfully applied for the synthesis of an imprinted polymer able to recognize organotin species. The synthesis has been accomplished by co-polymerization of the complex Bu(2)SnO-m-vinylbenzoin as the imprinting template plus co-monomer sodium methacrylate, and ethylene glycol dimethacrylate as cross-linker. The imprinting effect has been evidenced within the narrow pH range 2.5< pH< 3.5. At lower pH values, the imprinting effect is prevented by the exclusive existence of non-specific interactions, whereas pH>3.5 provokes a strong rebind of the template in both imprinted and non-imprinted polymers. This pH dependency can be explained as a selective chemical modification which reduces bind diversity following a model based on enolization by protonation of the specific cavities. Characterization of the adsorption isotherms showed good agreement with the Langmuir-Freundlich (LF) model, presenting quite homogeneous binding sites for a bulk material and high capacity in the imprinting pH range. In addition, the affinity spectrum (AS) method has been represented showing the typical profiles of LF isotherm for both sub-saturation and saturation levels, being in general agreement with the encountered values for fitting coefficients. The covalent molecular imprinted polymer has been successfully evaluated in a SPE process for further OTC determination in the certified mussel tissue (CRM 477).